Data Foundry

Medical device recalls 2016

ATEC CANISTER — Class II medical device recall Z-2239-2016

Terminated recall by Hologic, Inc, reported 2016-07-27, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Cracks ATEC Canister Lids.

Recall numberZ-2239-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHologic, Inc, Marlborough, MA, United States
Recall initiated2016-05-31
Classified2016-07-19
Reported by FDA2016-07-27
Terminated2017-05-24
DistributedAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
Countries outside the USAE, AR, AU, BE, CA, CH, CL, CO, DE, DK, FR, GB, HK, IE, IL, IT, KR, KW, LB, MY, NL, NZ, QA, SG, TH, TW, ZA
Quantity16,870
Reason classespackaging
Lot numbers20150013, 20150014

Product

ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast biopsy.

Reason for recall

Cracks ATEC Canister Lids.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2239-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.